ZIC2 Proteine
(ZIC2)
This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. This protein functions as a transcriptional repressor and may regulate tissue specific expression of dopamine receptor D1. Mutations in this gene cause holoprosencephaly type 5. Holoprosencephaly is the most common structural anomaly of the human brain. A polyhistidine tract polymorphism in this gene may be associated with increased risk of neural tube defects. This gene is closely linked to a gene encoding zinc finger protein of the cerebellum 5, a related family member on chromosome 13. [provided by RefSeq, Jul 2008].
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ZIC2
Spezies: Human
Wirt: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, SDS, WB
ZIC2
Spezies: Human
Wirt: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliase für ZIC2 Proteine
Zic family member 2 (ZIC2) Proteinezinc finger protein of the cerebellum 2 (Zic2) Proteine
Zic family member 2 (Zic2) Proteine
zic family member 2 (odd-paired homolog, Drosophila), a (zic2a) Proteine
Zic family member 2 L homeolog (zic2.L) Proteine
zic family member 2 (odd-paired homolog, Drosophila) b (zic2b) Proteine
cb851 Proteine
fb26a03 Proteine
hm:zeh0655 Proteine
HPE5 Proteine
hpe5 Proteine
id:ibd5017 Proteine
Ku Proteine
wu:fb26a03 Proteine
zic2 Proteine
zic2.1 Proteine
zic2.2 Proteine
zic2l Proteine
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